M. Horie et al., SIMULTANEOUS DETERMINATION OF 8 QUINOLONE ANTIBACTERIALS IN MEAT AND FISH BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Shokuhin Eiseigaku Zasshi, 36(1), 1995, pp. 62-67
A simple, rapid and reliable high performance liquid chromatographic (
HPLC) method for the simultaneous determination of eight quinolones (o
xolinic acid, nalidixic acid, flumequine, piromidic acid, benofloxacin
, danofloxacin, enrofloxacin and ofloxacin) in meat and fish has been
developed. The drugs were extracted with 0.2% metaphosphoric acid-acet
onitrile (7:3), followed by a Bond Elut C-18 clean-up procedure. The H
PLC separation was carried out on a Wakosil II 5C(18)-HG column (150x4
.6 mm i.d.) with 0.05M phosphate buffer (pH 2.5)-acetonitrile (65:35)
containing 3.5 mM sodium dodecyl sulfate (SDS) as the mobile phase at
a flow rate of 0.5 ml/min. The drugs were detected by UV detection (at
282 nm) and fluorescence detection (wavelength programing). The calib
ration graphs were rectilinear from 0.1 to 2 ng for danofloxacin, and
from 1 to 20 ng for other drugs. The recoveries of the drugs from meat
and fish fortified at the level of 0.2 mu g/g were 80.8 similar to 92
.1%, with high precision. The limit of detection was 0.01 mu g/g for e
ach drug. The method was applied in thermal stability studies of resid
ual oxolinic acid. The thermal stability of oxolinic acid was excellen
t.